Management of Acute Stroke Patients on Treatment with New Oral Anticoagulants: Addressing Real-world Anticoagulant Management Issues in Stroke (ARAMIS) Registry
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Cerebral InfarctionIch
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Age: Between 18 years - 120 years
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Gender: Male or Female
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Other Inclusion Criteria:
- Have been diagnosed with acute ischemic stroke and have been treated with dabigatran, rivaroxaban, apixaban, edoxaban within 7 days prior to admission, or
- Have been diagnosed with intracerebral hemorrhage and have been treated with warfarin or one of the new oral anticoagulants within 7 days prior to admission
- ARAMIS PRO follow-up study: Ability of patient or legally authorized representative to provide informed consent for longitudinal follow-up indicating they understand the purpose and the requirements of the study and are willing to participate.
You may not be eligible for this study if the following are true:
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- Patients who were transferred from another hospital or discharged to other acute care facility will be excluded.
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.